A hydrocarbon `A(C_4H_8)` on reaction with HCl gives a compound `B(C_4H_9Cl)` which on reaction with 1 mole of `NH_3` gives a compound `C(C_4H_(11)N)`. On reacting with `NaNO_2` and `HCl` followed by treatment with water, compound C yields an optically active alcohol,D. Ozonolysisi of A gives 2 moles of acetaldehyde.
The structure of compound C is

A hydrocarbon A(C_(4)H_(8)) on reaction with HCl gives a compound 'B' (C_(4)H_(9)Cl) which on reaction with 1 mole of NH_3 gives compound 'C' (C_(4)H_(11)N) . On reacting with NaN02 and HC1 followed by the'treatment with water, compound 'C yields an optically active alcohol, 'D'. Ozonolysis of 'A gives 2 moles of acetaldehyde. Identify compounds 'A to 'D'. Explain the reactions involved.

A hydrocarbon 'A' (C_(4)H_(8)) on reaction HCl gives a compound 'B', (C_(4)H_(9)Cl) which on reaction with 1 mol of NH_(3) gives compounds 'C' (C_(4)H_(11)N) . On reacting with NaNO_(2) and HCl followed by treatment with water compound 'C' yields an optically active alcohol, 'D'. Ozonolysis of 'A' given 2mols of acetyldehyde. Identify compound 'A' to 'D'. Explain the reaction involved.

A hydrocarbon 'A' (C_(4)H_(8)) on reaction HCl gives a compound 'B', (C_(4)H_(9)Cl) which on reaction with 1 mol of NH_(3) gives compounds 'C' (C_(4)H_(11)N) . On reacting with NaNO_(2) and HCl followed by treatment with water compound 'C' yields an optically active alcohol, 'D'. Ozonolysis of 'A' given 2mols of acetyldehyde. Identify compound 'A' to 'D'. Explain the reaction involved.

An organic compound A(C_(6)H_(7)N) on reaction with NaNO_(2)//HCl at 273-278 K following by warming with water gives B . B reacts with conc. HNO_(3) to give C . What is C ?